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Genome-wide association of early-onset myocardial...
Journal article

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Abstract

The Myocardial Infarction Genetics Consortium reports results of a genome-wide association study of early-onset myocardial infarction. The study analyzed common SNPs, common CNVs and rare CNVs and identified SNP alleles at three new loci associated with disease risk.

Authors

Kathiresan S; Voight BF; Purcell S; Musunuru K; Ardissino D; Mannucci PM; Anand S; Engert JC; Samani NJ; Schunkert H

Journal

Nature Genetics, Vol. 41, No. 3, pp. 334–341

Publisher

Springer Nature

Publication Date

January 1, 2009

DOI

10.1038/ng.327

ISSN

1061-4036

Associated Experts

Sonia Anand

Professor, Faculty of Health Sciences
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Labels

Fields of Research (FoR)

31 Biological Sciences3105 Genetics3001 Agricultural biotechnology3102 Bioinformatics and computational biology

Medical Subject Headings (MeSH)

AdultAge of OnsetAlgorithmsCase-Control StudiesFemaleGene DosageGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedMutationMyocardial InfarctionPolymorphism, Single NucleotideRisk Factors
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